100 recalls found for B. Braun Medical. Check if any of your products are affected.
B Braun Medical recalled its IV Administration Set used with Infusomat Space Large Volume Pumps and related models. The recall cites backflow of medication from secondary to primary IV containers and an occlusion that prevents priming. Hospitals and clinicians should stop using the device immediately and follow manufacturer recall instructions.
B. Braun Medical recalls 7,008 IV administration sets sold worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices may backflow from secondary to primary IV containers and may fail to prime. Hospitals and patients should stop using the sets and follow the manufacturer’s recall instructions.
B. Braun Medical recalled 1,250 IV administration sets distributed worldwide to hospitals and clinics. The devices may allow backflow of medication from secondary (piggyback) IV containers into primary containers and may not prime properly. Hospitals and other healthcare providers should stop using the devices immediately and follow recall instructions.
B Braun Medical recalled 41,976 IV Administration Sets sold worldwide after identifying a backflow risk. The device can allow medication to flow from secondary (piggyback) containers into the primary IV line and may not prime properly. Hospitals and healthcare providers should stop using the sets immediately and await recall instructions from B Braun Medical.
B Braun Medical recalls 12,200 IV administration sets sold to hospitals and medical distributors worldwide. The devices labeled NF1503 and catalog number 490062 may allow backflow of medication from secondary piggyback IV containers into primaries and may fail to prime. Hospitals should stop using the devices and follow the recall instructions.
B Braun Medical recalls 12,168 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The backflow of medication from secondary to primary containers and the inability to prime pose a high-risk issue. Stop using the device immediately and follow manufacturer instructions.
B. Braun Medical recalled 259,392 IV administration sets worldwide on Oct. 29, 2025. The devices could allow backflow of medication from secondary (piggyback) IV containers into primary IV containers and may not prime due to occlusion. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions in the notice.
B. Braun Medical Inc. recalled 5,952 IV Administration Sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore, for use with Infusomat Space, Outlook, and Vista Basic Pumps. The units carry Catalog Number 490612. The recall cites potential backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare teams
B Braun Medical recalled 98,568 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall covers catalog number 490274 and UDI-DI codes. The device presents a backflow risk and inability to prime. Hospitals and patients should stop using the device immediately and follow the manufacturer’s recall instructions.
B. Braun Medical has issued an active recall for 45,288 IV administration sets catalog 490412. The devices support gravity and pump-based IV administration with Infusomat Space, Outlook, and Vista Basic Pumps. The recall cites a design defect that can allow backflow from secondary piggyback containers into primary IV lines and prevent priming.
B Braun Medical Inc. recalls 36,936 IV administration sets used with Infusomat Space and other pumps worldwide. The recall was announced Oct. 29, 2025 and includes US and international distribution to Canada, Germany, Guatemala and Singapore. The devices may allow backflow of medication from secondary containers into the primary container and cannot be primed. Stop using immediately and follow the
B. Braun Medical recalled 122,232 IV administration sets sold worldwide through multiple medical distributors. The devices have a backflow risk from secondary (piggyback) IV containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the sets and follow the manufacturer's recall instructions.
B. Braun Medical recalled 66,792 IV Administration Sets sold worldwide through multiple healthcare distributors after reports of backflow and priming occlusion risk. The devices labeled catalog numbers 490241, 490298, and 490360 may allow medication to backflow from piggyback containers into primary lines and may fail to prime. Hospitals and clinicians should stop using immediately and follow the厂
B. Braun Medical recalled 3,120 IV administration sets distributed worldwide to hospitals and clinics. The recall concerns potential backflow of medication from secondary piggyback containers into primary containers and an inability to prime. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions issued by the manufacturer.
B Braun Medical recalled 24,624 Blood Administration Sets worldwide. The recall covers sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The risk involves backflow from secondary IV containers into primary containers and the inability to prime. Hospitals and clinics should stop using the devices immediately and follow recall instructions.
B. Braun Medical recalled 7,344 Blood Administration Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The devices may allow backflow from secondary (piggyback) IV containers into primary IV containers and cannot be primed. Hospitals and healthcare providers should stop using the devices immediately and follow manufacturer instructions.
BBraun Medical recalled 5,448 Blood Administration Sets used with Infusomat Space pumps worldwide sold to hospitals. The recall cites potential backflow of medication from secondary piggyback IV containers into primary IV containers and an inability to prime. Healthcare facilities should stop using the sets immediately and follow recall instructions from B. Braun Medical.
BBraun Medical recalled 12,700 ADDitIV gravity IV sets distributed worldwide. The sets can backflow medication from piggyback containers into primary IV containers and cannot be primed. Healthcare providers and patients should stop using the sets immediately and follow the recall instructions from BBraun Medical.
B Braun Medical Inc. recalled 100 units of the V1782F Univ IV Set W/0.2 MICRON FILTER, distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore. The sets may allow backflow from secondary piggyback IV containers into primary IV containers and cannot be primed. Healthcare facilities should stop using the devices immediately and follow the recall instructions.
B. Braun Medical recalled the Outlook IV Set 15DR W/2 CARESITE FILTER (Catalog 354214) used with Infusomat Space pumps and BBMI devices. The recall cites backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions by mail.